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Neurophysiological coding of space and time in the hippocampus, entorhinal cortex, and retrosplenial cortex

Neurophysiological recordings in behaving rodents demonstrate neuronal response properties that may code space and time for episodic memory and goal-directed behaviour. Here, we review recordings from hippocampus, entorhinal cortex, and retrosplenial cortex to address the problem of how neurons enco...

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Autores principales: Alexander, Andrew S., Robinson, Jennifer C., Dannenberg, Holger, Kinsky, Nathaniel R., Levy, Samuel J., Mau, William, Chapman, G. William, Sullivan, David W., Hasselmo, Michael E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7708714/
https://www.ncbi.nlm.nih.gov/pubmed/33294626
http://dx.doi.org/10.1177/2398212820972871
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author Alexander, Andrew S.
Robinson, Jennifer C.
Dannenberg, Holger
Kinsky, Nathaniel R.
Levy, Samuel J.
Mau, William
Chapman, G. William
Sullivan, David W.
Hasselmo, Michael E.
author_facet Alexander, Andrew S.
Robinson, Jennifer C.
Dannenberg, Holger
Kinsky, Nathaniel R.
Levy, Samuel J.
Mau, William
Chapman, G. William
Sullivan, David W.
Hasselmo, Michael E.
author_sort Alexander, Andrew S.
collection PubMed
description Neurophysiological recordings in behaving rodents demonstrate neuronal response properties that may code space and time for episodic memory and goal-directed behaviour. Here, we review recordings from hippocampus, entorhinal cortex, and retrosplenial cortex to address the problem of how neurons encode multiple overlapping spatiotemporal trajectories and disambiguate these for accurate memory-guided behaviour. The solution could involve neurons in the entorhinal cortex and hippocampus that show mixed selectivity, coding both time and location. Some grid cells and place cells that code space also respond selectively as time cells, allowing differentiation of time intervals when a rat runs in the same location during a delay period. Cells in these regions also develop new representations that differentially code the context of prior or future behaviour allowing disambiguation of overlapping trajectories. Spiking activity is also modulated by running speed and head direction, supporting the coding of episodic memory not as a series of snapshots but as a trajectory that can also be distinguished on the basis of speed and direction. Recent data also address the mechanisms by which sensory input could distinguish different spatial locations. Changes in firing rate reflect running speed on long but not short time intervals, and few cells code movement direction, arguing against path integration for coding location. Instead, new evidence for neural coding of environmental boundaries in egocentric coordinates fits with a modelling framework in which egocentric coding of barriers combined with head direction generates distinct allocentric coding of location. The egocentric input can be used both for coding the location of spatiotemporal trajectories and for retrieving specific viewpoints of the environment. Overall, these different patterns of neural activity can be used for encoding and disambiguation of prior episodic spatiotemporal trajectories or for planning of future goal-directed spatiotemporal trajectories.
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spelling pubmed-77087142020-12-07 Neurophysiological coding of space and time in the hippocampus, entorhinal cortex, and retrosplenial cortex Alexander, Andrew S. Robinson, Jennifer C. Dannenberg, Holger Kinsky, Nathaniel R. Levy, Samuel J. Mau, William Chapman, G. William Sullivan, David W. Hasselmo, Michael E. Brain Neurosci Adv Review Article Neurophysiological recordings in behaving rodents demonstrate neuronal response properties that may code space and time for episodic memory and goal-directed behaviour. Here, we review recordings from hippocampus, entorhinal cortex, and retrosplenial cortex to address the problem of how neurons encode multiple overlapping spatiotemporal trajectories and disambiguate these for accurate memory-guided behaviour. The solution could involve neurons in the entorhinal cortex and hippocampus that show mixed selectivity, coding both time and location. Some grid cells and place cells that code space also respond selectively as time cells, allowing differentiation of time intervals when a rat runs in the same location during a delay period. Cells in these regions also develop new representations that differentially code the context of prior or future behaviour allowing disambiguation of overlapping trajectories. Spiking activity is also modulated by running speed and head direction, supporting the coding of episodic memory not as a series of snapshots but as a trajectory that can also be distinguished on the basis of speed and direction. Recent data also address the mechanisms by which sensory input could distinguish different spatial locations. Changes in firing rate reflect running speed on long but not short time intervals, and few cells code movement direction, arguing against path integration for coding location. Instead, new evidence for neural coding of environmental boundaries in egocentric coordinates fits with a modelling framework in which egocentric coding of barriers combined with head direction generates distinct allocentric coding of location. The egocentric input can be used both for coding the location of spatiotemporal trajectories and for retrieving specific viewpoints of the environment. Overall, these different patterns of neural activity can be used for encoding and disambiguation of prior episodic spatiotemporal trajectories or for planning of future goal-directed spatiotemporal trajectories. SAGE Publications 2020-11-30 /pmc/articles/PMC7708714/ /pubmed/33294626 http://dx.doi.org/10.1177/2398212820972871 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Review Article
Alexander, Andrew S.
Robinson, Jennifer C.
Dannenberg, Holger
Kinsky, Nathaniel R.
Levy, Samuel J.
Mau, William
Chapman, G. William
Sullivan, David W.
Hasselmo, Michael E.
Neurophysiological coding of space and time in the hippocampus, entorhinal cortex, and retrosplenial cortex
title Neurophysiological coding of space and time in the hippocampus, entorhinal cortex, and retrosplenial cortex
title_full Neurophysiological coding of space and time in the hippocampus, entorhinal cortex, and retrosplenial cortex
title_fullStr Neurophysiological coding of space and time in the hippocampus, entorhinal cortex, and retrosplenial cortex
title_full_unstemmed Neurophysiological coding of space and time in the hippocampus, entorhinal cortex, and retrosplenial cortex
title_short Neurophysiological coding of space and time in the hippocampus, entorhinal cortex, and retrosplenial cortex
title_sort neurophysiological coding of space and time in the hippocampus, entorhinal cortex, and retrosplenial cortex
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7708714/
https://www.ncbi.nlm.nih.gov/pubmed/33294626
http://dx.doi.org/10.1177/2398212820972871
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